BioE Tissue
- Product NDC
- 57293-4424
- 11-digit product format
- 572934424
- Labeler code
- 57293
- Product ID
- 57293-4424_688bb4c0-7bc9-48ef-e053-2a91aa0ab7c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CALCIUM FLUORIDE, TRIBASIC CALCIUM PHOSPHATE, CALCIUM SULFATE ANHYDROUS, FERRUM PHOSPHORICUM, POTASSIUM CHLORIDE, DIBASIC POTASSIUM PHOSPHATE, POTASSIUM SULFATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE DIBASIC DIHYDRATE, SODIUM SULFATE ANHYDROUS, SILICON DIOXIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioEnergetics, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2000-10-28
- Marketing end
- 0000-00-00
- Substance
- CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; CALCIUM SULFATE ANHYDROUS; FERRUM PHOSPHORICUM; POTASSIUM CHLORIDE; DIBASIC POTASSIUM PHOSPHATE; POTASSIUM SULFATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM CHLORIDE; SODIUM PHOSPHATE DIBASIC DIHYDRATE; SODIUM SULFATE; SILICON DIOXIDE
- Active strength
- 12 [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57293-4424-2 | 57293442402 | 60 mL in 1 BOTTLE, GLASS (57293-4424-2) | 60 ml | 2000-10-28 | 0000-00-00 | No | No | Current |